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Amy |
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Woo |
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Senior Director, Clinical Operations |
Uniquity Bio |
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David |
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Crean |
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Managing Partner & Partner |
Cardiff Advisory LLC & 1004 Venture Partners |
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David H. Crean is a distinguished executive with over 30 years of experience across the life sciences and healthcare sectors with roles in strategic biopharma, private equity, venture capital, and investment banking. His career journey is a unique blend of scientific knowledge, business savvy, and financial leadership, which has earned him a reputation as a mentor, investor and dealmaker. Dr. Crean currently serves as the Founder and Managing Partner of Cardiff Advisory LLC, an M&A advisory firm, and is a Venture Partner at 1004 Venture Partners, a healthcare investment fund. He holds a Ph.D. in Biophysics and an M.S. in Oncology from the State University of New York Buffalo, as well as an MBA in Finance from Pepperdine University. |
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Elie |
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Arslan |
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Head, Quality, Principal Investigator and Program Management |
Cellics Therapeutics, Inc. |
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Compliance driven, highly successful Quality leader, with over 21 years of extensive experience in Quality in Biopharmaceuticals, Biologics, and Medical Devices. I am comprehensively knowledgeable and experienced in GxP (GMP, GLP and GCP), with an MBA and a Master of Science in Biotechnology from Johns Hopkins University. Elie oversees various Quality and Regulatory responsibilities and thrive in a fast-paced dynamic environment. Elie has 12 years of CMO experience, including experience in releasing drug substances, drug products, aseptic filling operations for clinical trials to commercial automated large-scale production, experience small molecules, large molecules, oncology and gene therapy. Elie successfully hosted FDA, CA FDB and QP inspections for PAI and routine Quality System inspections since 2015. |
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George |
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Ng |
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Chief Executive Officer |
Processa Pharmaceuticals |
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George Ng is a seasoned executive and entrepreneur in the life sciences industry, currently serving as Chief Executive Officer and Board Director at Processa Pharmaceuticals, Inc. (NASDAQ: PCSA) and as a partner at PENG Life Science Ventures (PENG LSV). Previously, he was President, COO, and Board Director at Calidi Biotherapeutics, Inc. (NYSE: CLDI), where he led the company’s successful public listing.
Mr. Ng co-founded Scilex Pharmaceuticals, Inc. (NASDAQ: SCLX), guiding it through product development, clinical trials, FDA approval, $140 million in financing, and its commercial launch and sale. His leadership career also includes senior executive roles at Sorrento Therapeutics, BioDelivery Sciences, Spectrum Pharmaceuticals, and Alpharma (now part of Pfizer), contributing to multiple successful drug product launches.
Before entering industry, Mr. Ng was a partner at two Am Law 200 firms, where he founded and led a national life sciences practice. He has served on the boards of several biotech companies and is a frequent speaker on legal, regulatory, and business topics.
Mr. Ng holds a Juris Doctor from the University of Notre Dame School of Law and a B.A.S. in Biochemistry and Economics from the University of California, Davis.
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Gregory |
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Opiteck |
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Vice President Head of Translational Sciences |
Allogene Therapeutics |
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An early adopter & advocate of precision medicine-driven clinical development, Greg has led mechanism‑based translational strategies that link drug design, human biology, and clinical data to inform decision-making in early development programs for over 25 years. He currently serves as Vice President, Head of Translational Medicine, at Janux Therapeutics here in San Diego, CA, where he oversees hypothesis‑driven translational and biomarker approaches supporting the clinical development of tumor‑activated T‑cell engager therapeutics. His work focuses on integrating pharmacology, immune activation, and on‑tumor biology to drive therapeutic activity & safety by explaining variance to treatment in indications such as metastatic castration‑resistant prostate cancer (mCRPC), including the lead JANX007 TCE program.
Prior to joining Janux, Greg was Vice President and Head of Precision and Translational Medicine at Affini-T Therapeutics and previously held roles of increasing responsibility in early clinical development at Receptos, Merck, and Bristol Myers Squibb. Greg earned his PhD from the University of North Carolina, Chapel Hill, and his BSc from the University of Notre Dame. |
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Jacqui |
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Blem |
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Vice President, Clinical Operations |
Wugen |
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Joseph |
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Shan |
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Vice President, Clinical Operations |
Adcentrx Therapeutics |
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Joseph (Joe) Shan, M.P.H., VP, Clinical Operations at Adcentrx Therapeutics, has nearly 30 years of clinical experience in biopharma and medical device companies. Nearly 25 years were focused on clinical development of oncology therapeutics, including radiopharmaceuticals, small molecules, targeted therapy, immunotherapy and cellular therapy. Prior to Adcentrx, Joe held leadership roles in Clinical Development Operations at Mosaic ImmunoEngineering, MEI Pharma, Elevar Therapeutics, Kiadis Pharma (formerly CytoSen Therapeutics) and was VP, Clinical & Regulatory Affairs and a corporate officer of Peregrine Pharmaceuticals for nearly a decade. Mr. Shan received his M.P.H. from George Washington University and B.S. from UCLA |
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Joe |
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Stalder |
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Executive Director Project Management |
Mirati Therapeutics |
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Joe Stalder is an Executive Director of Project Management at Mirati Therapeutics in San Diego, CA, co-founder of Groundswell Pharma Consulting, and editor of the book “Project Management for Drug Developers”. Joe has over 10 years of project management experience in pharmaceutical development in large and small companies. His experience includes Project Management department head, PMO head, and Lead Project Manager on several early- and late-stage development assets in oncology, infectious disease, cardiology, metabolism, and pulmonology. Joe is also a regular speaker at biopharma PPM conferences and is involved in biopharma PPM community organizations including PIPMG and BiopharmaPM. |
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John |
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Mattison |
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Former Operating Partner, Chief Medical Information Officer |
Arsenal Capital Partners |
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Matthew |
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Spear |
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Chief Development Officer / Chief Medical Officer |
Denovo Biopharma |
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Dr. Spear has been working in oncology and gene therapy research and development for over 30 years. He received a B.A. degree from Johns Hopkins University and an M.D. degree from Stanford University. Post-graduate training was in the Massachusetts General Hospital / Harvard University program. He has served as an Associate Professor on the faculty of the USC Keck School of Medicine, and the UCSD Medical School / UCSD Cancer Center where he managed a clinical practice, drug discovery/gene therapy research, and clinical trial programs for cancer. Dr. Spear led multiple oncology clinical development programs at Pfizer. He subsequently served as Chief Medical Officer and Senior Vice-President at Nereus Pharmaceuticals, followed by Head of Oncology and Head of Biotherapeutics at Sunovion Pharmaceuticals, then as a Vice-President at Incyte and Sangamo Therapeutics, and Chief Medical Officer at Poseida Therapeutics developing multiple CAR-T cell and gene therapy products. He is currently Chief Development Officer / Chief Medical Officer at Denovo Biopharma. He has also served as a CIRM CAR-T cell principal investigator, NIH / NCI study section, CPRIT grant review panel, biotechnology and pharmaceutical advisory boards, IRB/SRC, and scientific journal editorial review committees related to cancer and gene therapy, as well as authoring numerous scientific papers and patent applications.
CAR-T cell, RMAT, Gene Therapy, Gene Editing, AAV, HSV, transposon, hemophilia, Oncology, Hematology, NHL, myeloma, AML, MDS, prostate cancer, lung cancer, breast cancer, pancreatic cancer, GBM, H&N cancer, sarcoma, ovarian cancer, Oncolytic, Epigenetic, Biomarkers, Companion Diagnostics. Small Molecules, California Institute for Regenerative Medicine (CIRM), Immunotherapy, Vaccine, Antibody, Phage Display, sickle-cell, thalassemia, MPS I&II, MEK, PARP, CDK, VEGFR, Angiogenesis, VDA, HDAC, Proteosome, PI3K, BRD, JAK, PIM, FGFR, WT1, lysine-specific demethylase, OTC |
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Mehran |
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Moghaddam |
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CEO |
OROX Biosciences, Inc. |
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Dr. Mehran Moghaddam is the Founder and the Chief Executive Officer of OROX Biosciences, Inc., leading efforts to develop bifunctional small molecules for oncology and inflammatory diseases. With three decades of biopharmaceutical experience, he has guided research and development across multiple therapeutic areas, including oncology, fibrosis, cardiovascular, and CNS disorders. Mehran previously held key scientific and leadership roles at Celgene, DuPont, and Pfizer, contributing to the discovery and development of groundbreaking therapies such as Revlimid®, Pomalyst®, and Otezla®. |
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Kimberly |
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Ma |
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Senior Vice President, Clinical Development & Operations |
Abdera Therapeutics |
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